New oral drug chidamide tested for Hard-to-Treat bone marrow disorder

NCT ID NCT07616336

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This phase 2 trial tests the drug chidamide (Tucidinostat) in 15 people aged 60 or older with intermediate-to-high-risk myelodysplastic syndromes (MDS), a bone marrow disorder that can lead to leukemia. Participants take chidamide orally twice a week for up to 3 months. The study aims to see if the drug can improve blood counts and bone marrow health, and to check for side effects.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance
Chidamide (also called Tucidinostat), an oral drug
What this could lead to
If successful, this could point toward a new treatment option for people with intermediate-to-high-risk myelodysplastic syndromes who have few choices.
What could go wrong
This is a very small, early-phase trial with only 15 people. It may not show enough benefit or could have side effects that limit its use.

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Conditions

The condition(s) this trial relates to.

myelodysplastic syndrome Myelodysplastic Syndromes

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Zhongshan Hospital (Xiamen), Fudan University

    Xiamen, Fujian, 361015, China

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Other studies related to the condition(s) this trial covers.